A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5704117



Internal ID21730438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99224321..99224321hg38UCSC Ensembl
chr13:99876575..99876575hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17195637
Samples
Known GenesMIR548AN, UBAC2
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5704117
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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